Effects of oral HPΒCD-angiotensin-(1-7) supplementation on recreational mountain bike athletes: a crossover study.

Samara Silva de Moura, Francisco de Assis Dias Martins-Júnior, Emerson Cruz de Oliveira, Daniel Barbosa Coelho, Daniel Boari, Adriano Eduardo Lima-Silva, Daisy Motta-Santos, Robson Augusto Souza Dos Santos, Lenice Kappes Becker

Journal: The Physician and sportsmedicine 2024;52(1):65-76

PMID: 36752064

Abstract

BACKGROUND

Supplementation with Angiotensin-(1-7) [(Ang-1-7)] has received considerable attention due to its possible ergogenic effects on physical performance. The effects of a single dose of Ang-(1-7) on the performance of mountain bike (MTB) athletes during progressive load tests performed until the onset of voluntary fatigue have previously been demonstrated. This study tested the effects of Ang-(1-7) in two different exercise protocols with different metabolic demands: aerobic (time trial) and anaerobic (repeated sprint).

METHODS

Twenty one male recreational athletes were given capsules containing an oral formulation of HPβCD-Ang-(1-7) (0.8 mg) and HPβCD-placebo (only HPβCD) over a 7-day interval; a double-blind randomized crossover design was used. Physical performance was examined using two protocols: a 20-km cycling time trial or 4 × 30-s repeated all-out sprints on a leg cycle ergometer. Data were collected before and after physical tests to assess fatigue parameters, and included lactate levels, and muscle activation during the sprint protocol as evaluated by electromyography (EMG); cardiovascular parameters: diastolic and systolic blood pressure and heart rate; and performance parameters, time to complete (time trial), maximum power and mean power (repeated sprint).

RESULTS

Supplementation with an oral formulation of HPβCD-Ang-(1-7) reduced basal plasma lactate levels and promoted the maintenance of plasma glucose levels after repeated sprints. Supplementation with HPβCD-Ang-(1-7) also increased baseline plasma nitrite levels and reduced resting diastolic blood pressure in a time trial protocol. HPβCD-Ang-(1-7) had no effect on the time trial or repeat sprint performance, or on the EMG recordings of the vastus lateralis and vastus medialis.

CONCLUSIONS

Supplementation with HPβCD-Ang-(1-7) did not improve physical performance in time trial or in repeated sprints; however, it promoted the maintenance of plasma glucose and lactate levels after the sprint protocol and at rest, respectively. In addition, HPβCD-Ang-(1-7) also increased resting plasma nitrite levels and reduced diastolic blood pressure in the time trial protocol.

TRIAL REGISTRATION

RBR-2nbmpbc, registered January 6th, 2023. The study was prospectively registered.

Address: Health and Nutrition/PPGSN, Federal University of Ouro Preto, Ouro Preto, Brazil.; Physical Education School, Federal University of Ouro Preto, Ouro Preto, Brazil.; Biomedical Engineering, Federal University of ABC, São Paulo, Brazil.; Human Performance Research Group, Federal University of Technology Paraná, Curitiba, Brazil.; Department of Sports, School of Physical Education, Physiotherapy and Occupational Therapy, Federal University of Minas Gerais, Belo Horizonte, Brazil.; Department of Physiology and Biophysics, Federal University of Minas Gerais, and National Institute Science and Technology-NANOBIOPHAR-CNPQ/MCT, Belo Horizonte, Brazil.

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